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Pediatr Dermatol ; 40(3): 532-533, 2023.
Article in English | MEDLINE | ID: mdl-36382474

ABSTRACT

A healthy 12-month-old female presented with relapsing and remitting urticaria since birth that was resistant to treatment with antihistamines. A thorough history revealed extensive rheumatic disease on the father's side of the family, and subsequent genetic testing was positive for a missense variant of NLRP3, indicating cryopyrin-associated periodic fever syndrome (CAPS). CAPS encompasses a spectrum of diseases, all related to a defect in the same gene; manifestations vary in severity and presentation, but most are associated with recurrent rash and fever. Because the patient's only presenting symptom was rash, this case highlights the importance of having a high index of suspicion for cryopyrin-associated periodic fever syndrome in infants with persistent, early urticaria.


Subject(s)
Cryopyrin-Associated Periodic Syndromes , Exanthema , Urticaria , Infant , Humans , Female , NLR Family, Pyrin Domain-Containing 3 Protein/genetics , Mutation , Cryopyrin-Associated Periodic Syndromes/complications , Cryopyrin-Associated Periodic Syndromes/diagnosis , Cryopyrin-Associated Periodic Syndromes/drug therapy , Fever , Urticaria/diagnosis , Urticaria/drug therapy , Urticaria/etiology
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